GB819856A - Improvements relating to the production of cyanocarboxylic acid amides - Google Patents

Improvements relating to the production of cyanocarboxylic acid amides

Info

Publication number
GB819856A
GB819856A GB4103/58A GB410358A GB819856A GB 819856 A GB819856 A GB 819856A GB 4103/58 A GB4103/58 A GB 4103/58A GB 410358 A GB410358 A GB 410358A GB 819856 A GB819856 A GB 819856A
Authority
GB
United Kingdom
Prior art keywords
dinitrile
cyano
acid amides
exchanger
aqueous pyridine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB4103/58A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Inventa AG fuer Forschung und Patentverwertung
Original Assignee
Inventa AG fuer Forschung und Patentverwertung
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Inventa AG fuer Forschung und Patentverwertung filed Critical Inventa AG fuer Forschung und Patentverwertung
Publication of GB819856A publication Critical patent/GB819856A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Cyano-carboxylic acid amides are prepared by unilaterally hydrolysing a dinitrile of the general formula NC-(CX2)n-R-(CX2)m-CN, where R is an aromatic ring or a heterocyclic ring of aromatic character, where X is H, CH3 or C2H5 when the two substituents are not in ortho positions and where m and n are whole numbers including O by means of anion exchangers in the presence of a liquid containing water and a volatile base. The anion exchanger is preferably slightly cross-linked polystyrene of 1 to 7 per cent cross-linking which contains quaternary ammonium groups and the liquid is preferably aqueous pyridine or ammonia. The reaction may be carried out between 40 DEG and 100 DEG C. using about twice as much exchanger as dinitrile and the mixture, containing dissolved, suspended or emulsified dinitrile, stirred for several hours at the desired temperature. In the examples, cyano carboxamides together with some dicarboxamide and unchanged dinitrile are obtained when terephthalonitrile, isophthalonitrile, 2,6-dicyanopyridine and p-phenylene diacetic acid dinitrile are hydrolysed in the presence of aqueous pyridine. Specification 782,258 is referred to.
GB4103/58A 1957-03-08 1958-02-07 Improvements relating to the production of cyanocarboxylic acid amides Expired GB819856A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH819856X 1957-03-08

Publications (1)

Publication Number Publication Date
GB819856A true GB819856A (en) 1959-09-09

Family

ID=4539306

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4103/58A Expired GB819856A (en) 1957-03-08 1958-02-07 Improvements relating to the production of cyanocarboxylic acid amides

Country Status (1)

Country Link
GB (1) GB819856A (en)

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